Safety, Efficacy, and Survival Outcomes of Neoadjuvant/Induction Immunotherapy in Surgical and Radiotherapeutic Management of Non-Small Cell Lung Cancer: A Multicenter Real-World Study

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

This multicenter retrospective real-world study aims to evaluate the safety, efficacy and survival outcomes of neoadjuvant/induction immunotherapy in patients with non-small cell lung cancer (NSCLC). The study covers diverse treatment pathways, including surgery, definitive radiotherapy, and non-surgical strategies. It addresses gaps in existing trials by establishing a comprehensive cohort spanning neoadjuvant/induction therapy, perioperative management, and follow-up, providing real-world evidence to support treatment decisions in both operable and inoperable cases.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically confirmed non-small cell lung cancer (NSCLC), regardless of the presence of EGFR or ALK sensitive driver gene mutations;

• Clinical staging of IA-IIIC according to the AJCC 8th Edition before neoadjuvant treatment;

• Received at least one cycle of neoadjuvant immunotherapy (with or without chemotherapy);

• Assessed as resectable or potentially resectable by surgical experts prior to treatment.

Locations
Other Locations
China
Peking University Cancer Hospital & Institute
RECRUITING
Beijing
Peking University Third Hospital
RECRUITING
Beijing
Inner Mongolia Hospital of Peking University Cancer Hospital
RECRUITING
Hohhot
The Third Affliated Hospital of Kunming Medical University
RECRUITING
Kunming
Contact Information
Primary
Nan Wu, MD
nanwu@bjmu.edu.cn
0086-10-88196569
Time Frame
Start Date: 2024-12-01
Estimated Completion Date: 2028-03-31
Participants
Target number of participants: 500
Sponsors
Leads: Peking University Cancer Hospital & Institute

This content was sourced from clinicaltrials.gov